Application of 10071-38-2, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.10071-38-2, Name is 6-Chloro-2-methylpyridazin-3(2H)-one, molecular formula is C5H5ClN2O. In a article，once mentioned of 10071-38-2
The synthesis of four new series of acyclic heteroaromatic receptors is described. They are built by two flexible polyether chains functionalised at their end with pyridazinone or methylpyridazine rings and connected by pyridine or benzene units. Their ability as carriers of lipophilic and hydrophilic phenethylamines and metallic cations has been evaluated. Transport rates show that, in general, these compounds are much more efficient carriers of lipophilic amines than of dopamine and Na+, K+ and Ca2+ ions. Their transport selectivities towards phenethylamine and homoveratrylamine are discussed on the basis of their structural features. Molecular modelling studies suggest that interaction of the aromatic moiety of the guest with the pyridazinone rings via double pi-stacking, or with the pyridine ring by single pi-stacking, should be responsible of their enhanced efficacy and selectivity in the transport of lipophilic phenethylamines.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 10071-38-2
Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N1119 – PubChem